We took a multilevel developmental contextual approach and characterized trajectories of alcohol misuse from adolescence through early midlife, examined genetic and environmental contributions to individual differences in those trajectories, and identified adolescent and young adult factors associated with change in alcohol misuse. Data were from two longitudinal population-based studies. FinnTwin16 is a study of Finnish twins assessed at 16, 17, 18, 25, and 35 years (N = 5659; 52% female; 32% monozygotic). The National Longitudinal Study of Adolescent to Adult Health (Add Health) is a study of adolescents from the United States, who were assessed at five time points from 1994 to 2018 (N = 18026; 50% female; 64% White, 21% Black, 4% Native American, 7% Asian, 9% Other race/ethnicity). Alcohol misuse was measured as frequency of intoxication in FinnTwin16 and frequency of binge drinking in Add Health. In both samples, trajectories of alcohol misuse were best described by a quadratic growth curve: Alcohol misuse increased across adolescence, peaked in young adulthood, and declined into early midlife. Individual differences in these trajectories were primarily explained by environmental factors. Several adolescent and young adult correlates were related to the course of alcohol misuse, including other substance use, physical and mental health, and parenthood.

Beaks are one of the most important sclerochronological structures used to study the age and growth of cephalopods, in particular Octopus vulgaris Cuvier, 1797. The present study provides results of ageing of 128 O. vulgaris (56–239 mm dorsal mantle length, DML; 121–5974 g total weight, TW) collected in the southern Moroccan Mediterranean coasts between Fnideq and Jebha. The number of increments corresponding to the age (days since hatching) varied from 137–368 in females and from 129–382 in males. There was a significant correlation between beak and somatic growth. The correlation coefficients of the growth curves DML-Age and TW-Age were similar for both power and exponential models: DML = 0.185Age1.188 (R2 = 0.547), DML = 35.933e0.005Age (R2 = 0.546), TW = 0.00002Age3.260 (R2 = 0.532), TW = 29.56e0.014Age (R2 = 0.541). The average width of the increments was similar between females and males. It varied significantly with season and stage of sexual maturity. Comparison of the growth curve with those estimated by other authors showed that Moroccan Mediterranean O. vulgaris grew faster than that of Sardinia (Italy) and slower than that of the Mauritanian coast.

One of the largest nationwide bursts of the first COVID-19 outbreak occurred in Spain, where infection expanded in densely populated areas through March 2020. We analyse the cumulative growth curves of reported cases and deaths in all Spain and two highly populated regions, Madrid and Catalonia, identifying changes and sudden shifts in their exponential growth rate through segmented Poisson regressions. We associate these breakpoints with a timeline of key events and containment measures, and data on policy stringency and citizen mobility. Results were largely consistent for infections and deaths in all territories, showing four major shifts involving 19–71% reductions in growth rates originating from infections before 3 March and on 5–8, 10–12 and 14–18 March, but no identifiable effect of the strengthened lockdown of 29–30 March. Changes in stringency and mobility were only associated to the latter two shifts, evidencing an early deceleration in COVID-19 spread associated to personal hygiene and social distancing recommendations, followed by a stronger decrease when lockdown was enforced, leading to the contention of the outbreak by mid-April. This highlights the importance of combining public health communication strategies and hard confinement measures to contain epidemics.

The description of the growth of the Japanese quails is necessary to characterize the genetic potential of these birds raised in different countries. Thus, the aim of this study was to describe the genetic potential of Japanese quails by conducting a meta-analysis considering studies conducted in different countries. Only data about the subspecies Coturnix coturnix japonica were considered; studies regarding Coturnix coturnix coturnix were not examined. The criteria investigated were BW (W), age (t), year of publication and location of the study. Each set of genetic material within a publication was coded as one study. The Gompertz function was used to interpret the growth of laying quails; thus, each study was represented by Gompertz parameters. The W and t data were applied to estimate the values of Gompertz growth parameters, including BW at maturity (Wm), BW at birth (Wi), maturity rate (B) and inflection point (IP). The age at which the maximum growth rate was achieved (t*) was calculated considering the parameters Wm, Wi and B. To estimate these parameters, random regression was used to randomize the parameter Wm. The parameters estimated for each assay were used in exploratory, grouping, and principal component analyses. The values of Wi ranged from 4.1 to 11.6 g. The values of B ranged from 0.0393 to 0.1039/day, and consequently, the values of t* and IP ranged from 14 to 31 days and 9.21 to 31.03 g, respectively. These results show that there is considerable variability in the growth potential of Japanese quails. To better understand this variation, two groups were examined: Brazil and other countries, according to the grouping of Wi, Wm, B and t*; parameter B was the variable that presented the highest specificity, indicating that both groups modified the maturity rate. For the principal component analysis, the year of publication showed a relationship with the growth parameters but only for studies performed in Brazil. For studies carried out in other countries, the changes in growth parameters were not related to the year of publication. In Brazilian studies, there was a decrease in the maturity rate, but the weight at maturity was higher. Therefore, it appears that different strategies of genetic selection were adopted in Brazil compared to other countries.

For the management of mollusc resources, knowledge of various population parameters and exploitation level of the population of wedge clams are needed. Population dynamics on wedge clam, Donax scortum is still unknown in Asia. FAO-ICLARM Stock Assessment Tools (commonly known as FiSAT) was used for calculating population parameters of this species. The specimens of D. scortum were collected from Padukere sandy beach at monthly intervals from February 2009 to January 2010. Asymptotic length (Lα) was 70.88 mm and growth coefficient (K) was estimated at 0.64 year−1. The sizes attained by D. scortum were 33.51, 51.17, 60.49, 65.40, 67.99 and 69.36 mm at the end of first, second, third, fourth, fifth and sixth years of age, respectively. Density of clams ranged from 2 ind. m−2 (June, July and August) to 8 ind. m−2 (December). Biomass (total weight) of clams ranged between 10.084 g m−2 (August) to 185.100 g m−2 (December). Total mortality (Z) for D. scortum was 3.20 year−1. Natural mortality (M) and fishing mortality (F) were 0.64 year−1 and 2.56 year−1 respectively. Exploitation level (E) was computed as 0.80, indicating that the fishery of D. scortum in the coastal waters of Karnataka is overexploited.

Improvement of feed efficiency in pigs has been achieved essentially by increasing lean growth rate, which resulted in lower feed intake (FI). The objective was to evaluate the impact of strategies for improving feed efficiency on the dynamics of FI and growth in growing pigs to revisit nutrient recommendations and strategies for feed efficiency improvement. In 2010, three BWs, at 35±2, 63±9 and 107±7 kg, and daily FI during this period were recorded in three French test stations on 379 Large White and 327 French Landrace from maternal pig populations and 215 Large White from a sire population. Individual growth and FI model parameters were obtained with the InraPorc® software and individual nutrient requirements were computed. The model parameters were explored according to feed efficiency as measured by residual feed intake (RFI) or feed conversion ratio (FCR). Animals were separated in groups of better feed efficiency (RFI− or FCR−), medium feed efficiency and poor feed efficiency. Second, genetic relationships between feed efficiency and model parameters were estimated. Despite similar average daily gains (ADG) during the test for all RFI groups, RFI− pigs had a lower initial growth rate and a higher final growth rate compared with other pigs. The same initial growth rate was found for all FCR groups, but FCR− pigs had significantly higher final growth rates than other pigs, resulting in significantly different ADG. Dynamic of FI also differed between RFI or FCR groups. The calculated digestible lysine requirements, expressed in g/MJ net energy (NE), showed the same trends for RFI or FCR groups: the average requirements for the 25% most efficient animals were 13% higher than that of the 25% least efficient animals during the whole test, reaching 0.90 to 0.95 g/MJ NE at the beginning of the test, which is slightly greater than usual feed recommendations for growing pigs. Model parameters were moderately heritable (0.30±0.13 to 0.56±0.13), except for the precocity of growth (0.06±0.08). The parameter representing the quantity of feed at 50 kg BW showed a relatively high genetic correlation with RFI (0.49±0.14), and average protein deposition between 35 and 110 kg had the highest correlation with FCR (−0.76±0.08). Thus, growth and FI dynamics may be envisaged as breeding tools to improve feed efficiency. Furthermore, improvement of feed efficiency should be envisaged jointly with new feeding strategies.

The objective of this study was to estimate (co)variance components using random regression on B-spline functions to weight records obtained from birth to adulthood. A total of 82 064 weight records of 8145 females obtained from the data bank of the Nellore Breeding Program (PMGRN/Nellore Brazil) which started in 1987, were used. The models included direct additive and maternal genetic effects and animal and maternal permanent environmental effects as random. Contemporary group and dam age at calving (linear and quadratic effect) were included as fixed effects, and orthogonal Legendre polynomials of age (cubic regression) were considered as random covariate. The random effects were modeled using B-spline functions considering linear, quadratic and cubic polynomials for each individual segment. Residual variances were grouped in five age classes. Direct additive genetic and animal permanent environmental effects were modeled using up to seven knots (six segments). A single segment with two knots at the end points of the curve was used for the estimation of maternal genetic and maternal permanent environmental effects. A total of 15 models were studied, with the number of parameters ranging from 17 to 81. The models that used B-splines were compared with multi-trait analyses with nine weight traits and to a random regression model that used orthogonal Legendre polynomials. A model fitting quadratic B-splines, with four knots or three segments for direct additive genetic effect and animal permanent environmental effect and two knots for maternal additive genetic effect and maternal permanent environmental effect, was the most appropriate and parsimonious model to describe the covariance structure of the data. Selection for higher weight, such as at young ages, should be performed taking into account an increase in mature cow weight. Particularly, this is important in most of Nellore beef cattle production systems, where the cow herd is maintained on range conditions. There is limited modification of the growth curve of Nellore cattle with respect to the aim of selecting them for rapid growth at young ages while maintaining constant adult weight.

The availability of a population of mostly known-age African elephants Loxodonta africana from Amboseli National Park, Kenya, provided a unique opportunity to assess the use of dung bolus diameter for estimating age. A predictive equation for estimating dung bolus diameters from elephants of known age was derived and was found to follow the typical growth pattern exhibited by changes in shoulder height and foot length. The relationship between measurements of dung bolus and age was particularly strong when growth rates were high (age 0–25 years). The dung bolus growth curve from Amboseli elephants was similar to that derived from another wild population of African elephants, suggesting that dung bolus diameter can be used to assess age structure in areas where it is impossible to construct independent prediction curves of age and dung bolus.

The objective of the present study was to compare growth curves for live weight (LW) and body size of three strains of female dairy cattle reared under common environments in Ireland. One strain (HP) was selected from a predominantly North-American/European Holstein-Friesian genetic pool selected for high milk production. The second strain (HD) represented a predominantly North-American/European Holstein-Friesian genetic pool selected for high milk production but with greater selection emphasis on functional non-production traits. The third strain (NZ) consisted of New Zealand Holstein-Friesian females of high genetic merit for profitability in New Zealand. The data consisted of 99 animals (33 animals in each strain) with records on LW, length, girth and height from birth to a minimum of 594 days of age. The von Bertalanffy growth function was fitted to each animal's records separately and least-squares analyses were used to investigate the effect of strain on birth LW/body size, parameters of the growth function and average daily gains. Average mature live weight of the HD animals (591 kg) was significantly larger than that of the HP (566 kg) or NZ (543 kg) strain; the HD strain matured more slowly. The HD (134 cm) and HP (135 cm) strains were significantly taller than the NZ (128 cm) strain. Although the data set was relatively small there are indications that dairy females of North-American genetic origin were heavier at birth, grew faster, and were heavier and taller at maturity than dairy females of New Zealand origin.

Post-hatching changes in brain mass were investigated in mallards and four stocks of domesticated ducks, using growth curve analysis and allometry. The birds varied in age between hatching and 154 days. Percentage brain size at hatching in ducks varies between 22.5% and 28% which fits well into the precocial category. Brain growth shows a sigmoid course. The point of inflection is very early when compared to other organs. However, growth is slow after passing the growth rate maximum. Pekins show higher absolute brain masses than mallards. However, the growth patterns with respect to time are very similar among stocks. Strongly negative allometry is found with allometric exponents between 0.31 and 0.37 with the highest value in mallards. Allometrically, there is an increasing reduction of brain mass in Pekins when compared to mallards to about 12.5% in adults. No differences were found between mallards and either Muscovies or the Muscovy × Pekin cross. The reduction in relative brain size in domesticated animals when compared to their wild ancestors is generally attributed to a decrease in functional demands resulting from the artificial environment. Because brain growth is more conservative and less influenced by selection than body weight, we assume that this reduction is, at least in part, a result of the constancy of brain growth patterns.

The coypu (Myocastor coypus) is an aquatic rodent usually bred for fur production. Fluctuations in fur prices have led to coypu meat being considered as a genuine resource in commercial farms, which contribute to the diversification of agro-ecosystems. To characterize coypus as a meat resource, maternal and heterotic effects on birth weight, weaning weight, slaughter weight, number of days required to attain a weaning weight of l kg, and on two parameters of the Gompertz growth curve (asymptotic weight and maturing rate) were studied. Eight males and eight females of Standard (S) and Cognac (C) genotypes and of their reciprocal crosses (C × S) and (S × C), where the first letter denotes the paternal genotype, were used. Significant genotype, sex and (genotype × sex) interaction effects were evident for most traits. S animals were lighter than С at all ages. Hybrids with С mothers were heavier than their reciprocals. Maternal effects on the parameters of the growth curve were observed only in females. Heterotic effects were extremely significant. Favourable heterotic effects in immature animals were explained by a change in the F1 growth pattern. Males showed a dominant deviation toward low asymptotic weights and overdominance for high maturing rate. Females showed partial dominance of high asymptotic weight and over dominance for high maturing rate. This association of genetic effects would justify a productive system based on a terminal cross using С females and S males because of the higher maturing rate of both hybrids and the maternal effect of С genotype, a combination that allows higher weights at the usual slaughter age (6 months) or butchering of animals at earlier ages.

Protein accretion curves were derived using food intake, growth and body composition data from a total of 320 pigs, which comprised castrated males and gilts from five genotypes. The 32 pigs from each genotype/sex subclass were offered ad libitum a series of isoenergetic diets (13·8 MJ metabolizable energy per kg) designed to provide a non-limiting intake of nutrients and to allow maximum protein deposition rates. Four pigs from each subclass weren slaughtered at each of the live weights (kg) 25, 44, 65, 85, 100, 115, 130 and 150. Daily food intake (dF/dt) was described as an increasing exponential function of age (t), live weight (W) as an increasing exponential function of cumulative food consumed (F), and protein weight (Pr) as an allometric function of live weight (W). The rate of protein accretion in the body of pigs [d(Pr)/dt] was calculated as d(Pr)/dt = (dF/dt).(dW/dF).(dPr)/dW). Bootstrap procedures were used to estimate standard errors for the food intake, growth and compositional parameters and to obtain the confidence bands for the dependent variables (dF/dt, W, Pr and d(Pt)/dt).

Protein accretion rate as a function of live weight was curvilinear, increasing to a maximum, then decreasing with increasing live weight. There were significant differences between subclasses in the maximum rate of protein accretion, although there was no relationship between this rate and the live weight, stage of maturity, or age at which maximum protein accretion occurred. Describing protein accretion as a multiplicative function of food intake, food efficiency and the partitioning of nutrients in the body allowed changes in the magnitude and shape of the protein accretion curve to be ascribed to one, or a combination, of the above mechanisms.

Growth modelling was used to characterize the response to digestible lysine in two experiments (114 gilts in experiment 1 and 96 gilts in experiment 2) from 34 to 72·5 kg and 72·5 to 136 kg, respectively. Maize-soya-bean meal diets were formulated to assure that lysine (5·4 to 10·4 and 5·4 to 9·4 g digestible lysine per kg for experiments 1 and 2, respectively) was the first limiting amino acid. Analysis of variance was used to test linear and quadratic responses in cumulative weight gain on test as digestible lysine increased. A time × digestible lysine interaction (linear, P < 0·001) was detected, indicating that a separate regression equation for each lysine level was necessary. In experiment 1, average daily gain (ADG) and carcass crude protein (CP) accretion were maximized for gilts given 10·4, 9·4 and 8·4 g digestible lysine per kg from 34 to 44 kg, 44 to 54 kg, and 54 to 72·5 kg, respectively. Lipid accretion was minimized for gilts given 7·4 to 8·4 g digestible lysine per kg. In experiment 2, ADG was maximized by feeding 8·4 g/kg from 72·5 to 92·5 kg and 7·4 g/kg from 92·5 to 136 kg. Carcass CP accretion was maximized by feeding 9·4 g digestible lysine per kg, whereas lipid accretion was minimized for gilts given 8·4 g digestible lysine per kg from 72·5 to 136 kg. If feeding graded levels of digestible lysine resulted in parallel lines for protein accretion, mean values would result in accurate data evaluation. However, responses to digestible lysine changed over the feeding period. Therefore, the use of body weight and compositional growth curves offers an approach to more accurately characterize the growing pig's response to increased digestible lysine.

Growth results of 43 ostrich males and females were used to compile growth parameters of a flock that is representative of Oudtshoorn birds, using the Gompertz model. Growth results comprised 19 recordings of body weight for each individual commencing from 1-day-old to day 520. Individual fits of data to the growth model were exceptionally good, resulting in low CV values of 0·02 and 0·03 for the mean values of all estimates of mature live weight for male and females respectively. The estimated mean mature body weights for the flock were 119·2 kg for males and 122·3 kg for females. Rates of maturing were 9100 and 8500 for males and females respectively which corresponded to ages of 180·83 and 199·2 days at which maximum gain in weight were achieved. None of these parameter estimates differed significantly between sexes. Results in the present study suggested substantial adjustments to growth parameters for Oudtshoorn ostriches published by du Preez, Jarvis, Capatos and de Kock, 1992.